Analysis of Pseudomonas putida alkane-degradation gene clusters and flanking insertion sequences:: evolution and regulation of the alk genes

被引:225
作者
van Beilen, JB [1 ]
Panke, S [1 ]
Lucchini, S [1 ]
Franchini, AG [1 ]
Röthlisberger, M [1 ]
Witholt, B [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Biotechnol, CH-8093 Zurich, Switzerland
来源
MICROBIOLOGY-SGM | 2001年 / 147卷
关键词
alkane degradation; insertion sequence; chemotaxis; regulation;
D O I
10.1099/00221287-147-6-1621
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Pseudomonas putida GPo1 (commonly known as Pseudomonas oleovorans GPo1) alkBFGHJKL and alkST gene clusters, which encode proteins involved in the conversion of n-alkanes to fatty acids, are located end to end on the OCT plasmid, separated by 9.7 kb of DNA, This DNA segment encodes, amongst others, a methyl-accepting transducer protein (AlkN) that may be involved in chemotaxis to alkanes. In P, putida P1, the alkBFGHJKL and alkST gene clusters are flanked by almost identical copies of the insertion sequence ISPpu4 constituting a class 1 transposon. Other insertion sequences flank and interrupt the alk genes in both strains. Apart from the coding regions of the GPo1 and P1 alk genes (80-92 % sequence identity), only the alkB and alkS promoter regions are conserved. Competition experiments suggest that highly conserved inverted repeats in the alkS and alkS promoter regions bind AlkS.
引用
收藏
页码:1621 / 1630
页数:10
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